Cardiothoracic Systems, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K010117 | GUIDANT AXIUS CORONARY SHUNT | DXC | 2001-04-04 | View |
| 510(k) | K983270 | VOYAGER QUAD CANNULA | DWF | 1999-07-28 | View |
| 510(k) | K982419 | HEART-LIFT BALLOON POSITIONER | MWS | 1999-01-13 | View |
| 510(k) | K983135 | BLOWER/MISTER | FQH | 1998-11-13 | View |
| 510(k) | K963965 | CTS MIDCAB STITCHER | GEI | 1998-03-17 | View |
| 510(k) | K970638 | CTS MIDCAB FIXEDN DIAMETER CORONARY SHUNT | DXC | 1997-10-30 | View |
| 510(k) | K963503 | CTS MIDCAB CORONARY SHUNT | DXC | 1997-04-03 | View |
| 510(k) | K963930 | CTS MIDCAB/SVH BIPOLAR SCISSORS | GEI | 1997-01-16 | View |
No matching devices.
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